A Phase Ⅲ Clinical Study of HLX22 in Combination With Trastuzumab and Chemotherapy for the Treatment of Gastroesophageal Junction and Gastric Cancer

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorShanghai Henlius Biotech

About this trial

This is a double-blind, randomized, multiregion, comparative phase Ⅲ clinical study designed to evaluate the efficacy and safety of HLX22 in combination with trastuzumab and chemotherapy as first-line treatment in patients with HER2-positive locally advanced/metastatic adenocarcinoma of the gastric and/or gastroesophageal junction (G/GEJ).Eligible subjects will be randomized to the two groups based on a 1:1 ratio. Enrolled subjects shall be treated with the study drug until the loss of clinical benefit, death, intolerable toxicity, withdrawal of informed consent, or other reasons specified by the protocol (whichever occurs first).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male/female who are at least 18 years of age on the day of signing the informed consent.

With histologically or cytologically confirmed diagnosis of previously untreated, locally advanced unresectable or metastatic HER2-positive gastric or gastroesophageal junction adenocarcinoma.

Had measurable disease as assessed by IRRC according to the RECIST v1.1, the target lesion must not be a bone metastatic lesion only.

HER2-positive tumor defined as either IHC 3+ or IHC 2+ in combination with ISH+ or FISH, as assessed by a central laboratory on a primary or metastatic tumor.

Disqualifiers

Patients with other malignant tumors within 2 years before the randomization.

Evidence of disease progression within 6 months (before randomization) after completion of prior neoadjuvant or adjuvant chemotherapy (or both) or radiotherapy for gastric adenocarcinoma or gastroesophageal junction adenocarcinoma.

Previous treatment with any HER2-target therapy.

Active gastrointestinal bleeding

Trial design

Design model

Parallel

Treatments tested in this trial

  • HLX22

    Drug

    HLX22 15mg/kg Q3w

  • Pembrolizumab

    Drug

    Pembrolizumab 200mg q3w

  • Trastuzumab

    Drug

    Trastuzumab 8 mg/kg loading dose and then 6 mg/kg maintenance thereafter ,Q3W

  • Oxaliplatin

    Drug

    Oxaliplatin 130 mg/m2 ,Q3W

  • Capecitabine

    Drug

    Capecitabine 1000 mg/m2 bid on Days 1-14 ,Q3W

Treatment groups

550 Participants
are divided into 2 treatment groups
Group A: Experimental groupExperimental treatment 4 interventions
Group B: Control groupActive comparator 4 interventions

Trial outcomes

Primary outcomes

1

Progression-Free Survival (PFS)per RECIST 1.1 assessed by IRRC(Independent Radiology Review Committee)

PFS is defined as the time from randomization to the first documented disease progression per RECIST 1.1 or death due to any cause, whichever occurs first. PFS will be determined for each treatment arm

Time frame
Up to 5 years
2

Overall Survival (OS)

OS is defined as the time from randomization to death due to any cause. OS will be determined for each treatment arm.

Time frame
Up to 5 years

Secondary outcomes

1

PFS per RECIST 1.1 assessed by investigator

PFS is defined as the time from randomization to the first documented disease progression per RECIST 1.1 or death due to any cause, whichever occurs first. PFS will be determined for each treatment arm

Time frame
Up to 5 years
2

Objective Response Rate (ORR) assessed by IRRC and investigator per RECIST v1.1

ORR is defined as the percentage of participants who have a Complete Response (\[CR\], disappearance of all evidence of disease) or Partial Response (\[PR\], regression of measurable disease and no new sites) per RECIST 1.1. ORR will be determined for each treatment arm.

Time frame
Up to 5 years
3

Adverse events (AE)

An AE is any untoward medical occurrence in a participant that is temporally associated with the use of study treatment, whether or not considered related to the study treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal laboratory finding), symptom, or disease (new or exacerbated) temporally associated with the use of a study treatment. The number of participants who experience an AE will be reported for each treatment arm.

Time frame
Up to 5 years

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.